but happy to get a picture on way to hospital to see Mum's Consultant.
Monday, June 18, 2007
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Maggie at Port Eliot
Maggie at Port Eliot
About Me
- Maggie
- I've had ME/CFS since March 9th 1992. I am lucky that I got an early diagnosis, and also that I was advised to rest as much as I needed to. My belief is that because of that I am far less disabled than I might have been... I can garden still to a limited extent (hubby does all the hard work and I do the fiddly bits) and I'm rediscovering drawing, knitting, and my love of spinning and textiles.
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1 comment:
Oh Maggie, I've just been over to Mary's to read about the meeting and it sounds ghastly. Sounds all too familiar though.
If the Home will accept people like your Mum (if they're geared up for it in terms of staff and expertise) it may be the best thing to put Mum and Dad together. Maybe they could have a room together or next to each other. I've seen that work well before. It would also mean that for you, you wouldn't have to shuttle between 2 locations when visiting (we had to do that and it was exhausting).
I do hope things can be worked out soon. Get all the help you can and lean on the Social Workers as much as poss. Are you in touch with your local Alzheimer's group ? -- they can be very helpful and supportive with all sorts of confusion and dementia issues -- not just classic Alz. Also try Age Concern and see if they have a dedicated dementia support team.
Thinking of you.
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